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1.
Pediatr Radiol ; 49(9): 1185-1191, 2019 08.
Article in English | MEDLINE | ID: mdl-31152212

ABSTRACT

BACKGROUND: Bone age determination is usually employed to evaluate growth disorders and their treatment. The Greulich-Pyle method is the simplest and most frequently used type of evaluation, but it presents huge interobserver variability. The BoneXpert is a computer-automated method developed to avoid significant bone age variability among distinct observers. OBJECTIVE: To compare the BoneXpert and Greulich-Pyle methods of bone age determination in eutrophic children and adolescents, as well as in overweight and obese pediatric patients. MATERIALS AND METHODS: The sample comprised 515 participants, 253 boys (159 eutrophic, 53 overweight and 41 obese) and 262 girls (146 eutrophic, 76 overweight and 40 obese). Left hand and wrist radiographs were acquired for bone age determination using both methods. RESULTS: There was a positive correlation between chronological age and Greulich-Pyle, chronological age and BoneXpert, and Greulich-Pyle and BoneXpert. There was a significant increase (P<0.05) in bone age in both the Greulich-Pyle and BoneXpert methods in obese boys when compared to eutrophic or overweight boys of the same age. In girls, there was an increase in bone age in both obese and overweight individuals when compared to eutrophic girls (P<0.05). The Greulich-Pyle bone age was advanced in comparison to that of BoneXpert in all groups, except in obese boys, in which bone age was similarly advanced in both methods. CONCLUSION: The BoneXpert computer-automated bone age determination method showed a significant positive correlation with chronological age and Greulich-Pyle. Furthermore, the impact of being overweight or obese on bone age could be identified by both methods.


Subject(s)
Age Determination by Skeleton/methods , Obesity , Overweight , Thinness , Adolescent , Brazil , Child , Child, Preschool , Cross-Sectional Studies , Female , Hand/diagnostic imaging , Humans , Male , Prospective Studies , Wrist/diagnostic imaging
2.
Rev. bras. otorrinolaringol ; 71(2): 237-240, mar.-abr. 2005. ilus
Article in Portuguese | LILACS | ID: lil-408699

ABSTRACT

Paragangliomas são neoplasias que surgem a partir do tecido paragangliônico do sistema nervoso autônomo. Os paragangliomas da cabeca e pescoco são bastante raros. Os tipos mais freqüentemente encontrados são o carotídeo, o júgulo-timpânico e o vagal. Paragangliomas do nariz e dos seios paranasais são muito infreqüentes. Os autores descrevem um caso de paraganglioma nasal em um paciente do sexo masculino, com 45 anos de idade, que foi submetido à exérese da lesão, e relatam os achados clínicos, critérios diagnósticos, tratamento, prognóstico e revisão da literatura. Consideramos importante o relato deste caso em vista da raridade da localizacão nasal dos paragangliomas.


Subject(s)
Humans , Male , Middle Aged , Nose Neoplasms/diagnosis , Paraganglioma/diagnosis , Nose Neoplasms/surgery , Paraganglioma/surgery
3.
Braz J Otorhinolaryngol ; 71(2): 237-40, 2005.
Article in English | MEDLINE | ID: mdl-16450456

ABSTRACT

Paragangliomas are tumors of the autonomic nervous system, arising from paraganglionic tissue. Paragangliomas of the head and neck region are very rare. In the head and neck, the most common sites of origin of this neoplasm are the carotid body, the jugular bulb and the vagal body. Paragangliomas of the nose and paranasal sinuses are very uncommon. The authors referred one case of nasal paraganglioma in a 45-year-old male patient, who was submitted to surgical excision, and included clinical findings, diagnostic criteria, treatment, prognosis and literature review. The importance of reporting this case refers to the rare incidence of paragangliomas in the nasal cavity and paranasal sinuses.


Subject(s)
Nose Neoplasms , Paraganglioma , Humans , Male , Middle Aged , Nose Neoplasms/diagnosis , Nose Neoplasms/surgery , Paraganglioma/diagnosis , Paraganglioma/surgery
4.
Rev. bras. otorrinolaringol ; 70(3)maio-jun. 2004. ilus
Article in Portuguese | LILACS | ID: lil-363018

ABSTRACT

As neoplasias nasais são bastante raras. Os tumores mais observados na cavidade nasal são papilomas epiteliais, angiomas, carcinoma de células transicionais, carcinoma pavimentoso e adenocarcinoma. O adenoma pleomórfico pertence ao grupo de tumores que aparecem com menor freqüência na fossa nasal, e é o tumor benigno glandular mais comum originado na cabeça e pescoço. A apresentação clínica típica dos pacientes com adenoma pleomórfico do septo nasal é de obstrução nasal unilateral, epistaxe e massa indolor na cavidade nasal. Em vista da raridade da apresentação clínica do adenoma pleomórfico nesta localização, os autores descrevem um caso de adenoma pleomórfico nasal em um paciente do sexo masculino, com 69 anos de idade, onde relatam os achados clínicos, critérios diagnósticos, tratamento, prognóstico e revisão da literatura.

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